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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">rsp</journal-id><journal-title-group><journal-title xml:lang="ru">Научно-практическая ревматология</journal-title><trans-title-group xml:lang="en"><trans-title>Rheumatology Science and Practice</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1995-4484</issn><issn pub-type="epub">1995-4492</issn><publisher><publisher-name>IMA-PRESS, LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.47360/1995-4484-2020-544-549</article-id><article-id custom-type="elpub" pub-id-type="custom">rsp-2958</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОРЫ И ЛЕКЦИИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS AND LECTURES</subject></subj-group></article-categories><title-group><article-title>Первичная гипертрофическая остеоартропатия</article-title><trans-title-group xml:lang="en"><trans-title>Primary hypertrophic osteoarthropathy</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4168-7219</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Трисветова</surname><given-names>Е. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Trisvetova</surname><given-names>E. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Трисветова Евгения Леонидовна</p><p>220116, Минск, пр. Дзержинского, д. 83</p></bio><bio xml:lang="en"><p>Evgenia L. Trisvetova</p><p>220116, Minsk, Dzerzhinsky Ave., 83</p></bio><email xlink:type="simple">trisvet-47@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>УО «Белорусский государственный медицинский университет»</institution><country>Беларусь</country></aff><aff xml:lang="en"><institution>Belarusian State Medical University</institution><country>Belarus</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>09</day><month>11</month><year>2020</year></pub-date><volume>58</volume><issue>5</issue><fpage>544</fpage><lpage>549</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Трисветова Е.Л., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Трисветова Е.Л.</copyright-holder><copyright-holder xml:lang="en">Trisvetova E.L.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://rsp.mediar-press.net/rsp/article/view/2958">https://rsp.mediar-press.net/rsp/article/view/2958</self-uri><abstract><p>Представлены сведения о редком наследственном заболевании – первичной гипертрофической остеоартропатии с аутосомно-доминантным и аутосомно-рецессивным наследованием. Генетическая гетерогенность обусловливает клинический полиморфизм симптомов, появляющихся в детском и подростковом возрасте. Дифференциальную диагностику необходимо проводить со вторичной гипертрофической остеоартропатией, встречающейся в 90% случаев и ассоциированной со злокачественными новообразованиями, ревматическими болезнями и другими заболеваниями. Важное значение отводится рентгенологическим признакам, позволяющим уточнить локализацию, протяженность и характер поражения костей. Специфическое лечение заболевания отсутствует.</p></abstract><trans-abstract xml:lang="en"><p>The article presents information about a rare hereditary disease – primary hypertrophic osteoarthropathy with autosomal dominant and autosomal recessive inheritance. Genetic heterogeneity is responsible for the clinical polymorphism of symptoms that appear in childhood and adolescence. Differential diagnosis should be carried out with secondary hypertrophic osteoarthropathy, which occurs in 90% of cases and is associated with malignant neoplasms, rheumatic diseases and other diseases. X-ray signs are of great importance to clarify the localization, extent and nature of bone lesions. There is no specific treatment for the disease.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>гипертрофическая остеоартропатия</kwd><kwd>первичная</kwd><kwd>вторичная</kwd><kwd>диагностика</kwd><kwd>дифференциальная диагностика</kwd></kwd-group><kwd-group xml:lang="en"><kwd>hypertrophic osteoarthropathy</kwd><kwd>primary</kwd><kwd>secondary</kwd><kwd>diagnosis</kwd><kwd>differential diagnosis</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Castori M., Sinibaldi L., Mingarelli R., et al. Pachydermoperiostosis: an update. Clin Genet. 2005;68(6):477–486. 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